Cargando…
Experimentally constrained CA1 fast-firing parvalbumin-positive interneuron network models exhibit sharp transitions into coherent high frequency rhythms
The coupling of high frequency oscillations (HFOs; >100 Hz) and theta oscillations (3–12 Hz) in the CA1 region of rats increases during REM sleep, indicating that it may play a role in memory processing. However, it is unclear whether the CA1 region itself is capable of providing major contributi...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3804767/ https://www.ncbi.nlm.nih.gov/pubmed/24155715 http://dx.doi.org/10.3389/fncom.2013.00144 |
_version_ | 1782288206673215488 |
---|---|
author | Ferguson, Katie A. Huh, Carey Y. L. Amilhon, Bénédicte Williams, Sylvain Skinner, Frances K. |
author_facet | Ferguson, Katie A. Huh, Carey Y. L. Amilhon, Bénédicte Williams, Sylvain Skinner, Frances K. |
author_sort | Ferguson, Katie A. |
collection | PubMed |
description | The coupling of high frequency oscillations (HFOs; >100 Hz) and theta oscillations (3–12 Hz) in the CA1 region of rats increases during REM sleep, indicating that it may play a role in memory processing. However, it is unclear whether the CA1 region itself is capable of providing major contributions to the generation of HFOs, or if they are strictly driven through input projections. Parvalbumin-positive (PV+) interneurons may play an essential role in these oscillations due to their extensive connections with neighboring pyramidal cells, and their characteristic fast-spiking. Thus, we created mathematical network models to investigate the conditions under which networks of CA1 fast-spiking PV+ interneurons are capable of producing high frequency population rhythms. We used whole-cell patch clamp recordings of fast-spiking, PV+ cells in the CA1 region of an intact hippocampal preparation in vitro to derive cellular properties, from which we constrained an Izhikevich-type model. Novel, biologically constrained network models were constructed with these individual cell models, and we investigated networks across a range of experimentally determined excitatory inputs and inhibitory synaptic strengths. For each network, we determined network frequency and coherence. Network simulations produce coherent firing at high frequencies (>90 Hz) for parameter ranges in which PV-PV inhibitory synaptic conductances are necessarily small and external excitatory inputs are relatively large. Interestingly, our networks produce sharp transitions between random and coherent firing, and this sharpness is lost when connectivity is increased beyond biological estimates. Our work suggests that CA1 networks may be designed with mechanisms for quickly gating in and out of high frequency coherent population rhythms, which may be essential in the generation of nested theta/high frequency rhythms. |
format | Online Article Text |
id | pubmed-3804767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-38047672013-10-23 Experimentally constrained CA1 fast-firing parvalbumin-positive interneuron network models exhibit sharp transitions into coherent high frequency rhythms Ferguson, Katie A. Huh, Carey Y. L. Amilhon, Bénédicte Williams, Sylvain Skinner, Frances K. Front Comput Neurosci Neuroscience The coupling of high frequency oscillations (HFOs; >100 Hz) and theta oscillations (3–12 Hz) in the CA1 region of rats increases during REM sleep, indicating that it may play a role in memory processing. However, it is unclear whether the CA1 region itself is capable of providing major contributions to the generation of HFOs, or if they are strictly driven through input projections. Parvalbumin-positive (PV+) interneurons may play an essential role in these oscillations due to their extensive connections with neighboring pyramidal cells, and their characteristic fast-spiking. Thus, we created mathematical network models to investigate the conditions under which networks of CA1 fast-spiking PV+ interneurons are capable of producing high frequency population rhythms. We used whole-cell patch clamp recordings of fast-spiking, PV+ cells in the CA1 region of an intact hippocampal preparation in vitro to derive cellular properties, from which we constrained an Izhikevich-type model. Novel, biologically constrained network models were constructed with these individual cell models, and we investigated networks across a range of experimentally determined excitatory inputs and inhibitory synaptic strengths. For each network, we determined network frequency and coherence. Network simulations produce coherent firing at high frequencies (>90 Hz) for parameter ranges in which PV-PV inhibitory synaptic conductances are necessarily small and external excitatory inputs are relatively large. Interestingly, our networks produce sharp transitions between random and coherent firing, and this sharpness is lost when connectivity is increased beyond biological estimates. Our work suggests that CA1 networks may be designed with mechanisms for quickly gating in and out of high frequency coherent population rhythms, which may be essential in the generation of nested theta/high frequency rhythms. Frontiers Media S.A. 2013-10-22 /pmc/articles/PMC3804767/ /pubmed/24155715 http://dx.doi.org/10.3389/fncom.2013.00144 Text en Copyright © 2013 Ferguson, Huh, Amilhon, Williams and Skinner. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Ferguson, Katie A. Huh, Carey Y. L. Amilhon, Bénédicte Williams, Sylvain Skinner, Frances K. Experimentally constrained CA1 fast-firing parvalbumin-positive interneuron network models exhibit sharp transitions into coherent high frequency rhythms |
title | Experimentally constrained CA1 fast-firing parvalbumin-positive interneuron network models exhibit sharp transitions into coherent high frequency rhythms |
title_full | Experimentally constrained CA1 fast-firing parvalbumin-positive interneuron network models exhibit sharp transitions into coherent high frequency rhythms |
title_fullStr | Experimentally constrained CA1 fast-firing parvalbumin-positive interneuron network models exhibit sharp transitions into coherent high frequency rhythms |
title_full_unstemmed | Experimentally constrained CA1 fast-firing parvalbumin-positive interneuron network models exhibit sharp transitions into coherent high frequency rhythms |
title_short | Experimentally constrained CA1 fast-firing parvalbumin-positive interneuron network models exhibit sharp transitions into coherent high frequency rhythms |
title_sort | experimentally constrained ca1 fast-firing parvalbumin-positive interneuron network models exhibit sharp transitions into coherent high frequency rhythms |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3804767/ https://www.ncbi.nlm.nih.gov/pubmed/24155715 http://dx.doi.org/10.3389/fncom.2013.00144 |
work_keys_str_mv | AT fergusonkatiea experimentallyconstrainedca1fastfiringparvalbuminpositiveinterneuronnetworkmodelsexhibitsharptransitionsintocoherenthighfrequencyrhythms AT huhcareyyl experimentallyconstrainedca1fastfiringparvalbuminpositiveinterneuronnetworkmodelsexhibitsharptransitionsintocoherenthighfrequencyrhythms AT amilhonbenedicte experimentallyconstrainedca1fastfiringparvalbuminpositiveinterneuronnetworkmodelsexhibitsharptransitionsintocoherenthighfrequencyrhythms AT williamssylvain experimentallyconstrainedca1fastfiringparvalbuminpositiveinterneuronnetworkmodelsexhibitsharptransitionsintocoherenthighfrequencyrhythms AT skinnerfrancesk experimentallyconstrainedca1fastfiringparvalbuminpositiveinterneuronnetworkmodelsexhibitsharptransitionsintocoherenthighfrequencyrhythms |